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  • 1
    Publication Date: 1993-06-01
    Print ISSN: 0168-2563
    Electronic ISSN: 1573-515X
    Topics: Chemistry and Pharmacology , Geosciences
    Published by Springer
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  • 2
    Publication Date: 1992-01-01
    Print ISSN: 0168-2563
    Electronic ISSN: 1573-515X
    Topics: Chemistry and Pharmacology , Geosciences
    Published by Springer
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Biogeochemistry 17 (1992), S. 123-143 
    ISSN: 1573-515X
    Keywords: freshwater ; sulfate reduction ; sulfur oxidation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract In an oligotrophic moorland pool in The Netherlands, S cycling near the sediment/water boundary was investigated by measuring (1) SO4 2− reduction rates in the sediment, (2) depletion of SO4 2− in the overlying water column and (3) release of35S from the sediment into the water column. Two locations differing in sediment type (highly organic and sandy) were compared, with respect to reduction rates and depletion of SO4 2− in the overlying water. Sulfate reduction rates in sediments of an oligotrophic moorland pool were estimated by diagenetic modelling and whole core35SO4 2− injection. Rates of SO4 2− consumption in the overlying water were estimated by changes in SO4 2− concentration over time in in situ enclosures. Reduction rates ranged from 0.27–11.2 mmol m−2 d−1. Rates of SO4 2− uptake from the enclosed water column varied from −0.5, −0.3 mmol m−2 d−1 (November) to 0.43–1.81 mmol m−2 d−1 (July, August and April). Maximum rates of oxidation to SO4 2− in July 1990 estimated by combination of SO4 2− reduction rates and rates of in situ SO4 2− uptake in the enclosed water column were 10.3 and 10.5 mmol m−2 d−1 at an organic rich and at a sandy site respectively. Experiments with35S2− and35SO4 2− tracer suggested (1) a rapid formation of organically bound S from dissimilatory reduced SO4 2− and (2) the presence of mainly non SO4 2−-S derived from reduced S transported from the sediment into the overlying water. A35S2− tracer experiment showed that about 7% of35S2− injected at 1 cm depth in a sediment core was recovered in the overlying water column. Sulfate reduction rates in sediments with higher volumetric mass fraction of organic matter did not significantly differ from those in sediments with a lower mass fraction of organic matter.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-9729
    Keywords: freshwater ; moorland ; pool ; S budgets
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Energy, Environment Protection, Nuclear Power Engineering , Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition
    Notes: Abstract The chemical composition of surface waters of two Dutch moorland pools and of incident precipitation, was monitored from 1982 to 1990. For this period, sulfur and water budgets were calculated using a hydrochemical model developed for well-mixed non-stratifying lakes. Total atmospheric deposition of S decreased significantly after 1986 at both locations. A model describing the sulfur budget in terms of input, output and reduction/oxidation processes predicted a fast decrease of pool water SO4 2− concentrations after a decrease of atmospheric input. However, SO4 2− concentrations in the surface water was lowered only slightly or remained constant. Apparently a source within the lake caused the unexpectedly high SO4 2− concentrations. The possible supply of SO4 2− from the sediment through regulation by (K-)Al-SO4 containing minerals or desorption of SO4 2− from positively charged surfaces in the sediment was evaluated. Solubility calculations of pore water with respect to alunite, basaluminite and jurbanite indicated that SO4 2− concentration was not regulated by these minerals. It is suggested here (1) that desorption of SO4 2− from peaty sediments may account for the estimated SO4 2− supply provided that the adsorption complex is periodically recharged by partial oxidation of the upper bottom sediments and (2) that because of exposure of a part of the pool bottom to the atmosphere during dry summers and subsequent oxidation of reduced S, the amount of SO4 2− may be provided which complements the decreasing depositional SO4 2− input. In future research these two mechanisms need to be investigated.
    Type of Medium: Electronic Resource
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